Some advice for ‘long Covid’ sufferers, from the chronic fatigue community

A young woman lies on a couch with her back to the camera, while a cute Golden retriever dog lies over her.

Understanding the connection between chronic fatigue syndrome and ‘long Covid’ might be helpful in treating symptoms that doctors will find all too easy to dismiss. When people began to report signs of “long Covid”, characterised by a lack of full recovery from the virus and debilitating fatigue, I recognised their stories. Not the Covid itself, … Read more

Women, pain and anti-vaxxers: Why medicine is due for a feminist reckoning

Gabrielle Jackson is a Sydney-based Guardian journalist who has written a book about her pain, and the pain of women, and the ways in which the medical system is making it worse. The book is called Pain and Prejudice: a call to arms for women and their bodies. It focuses on ‘women’s troubles’ – a … Read more

Inventing illness? What it’s like when your GP won’t believe you’re in pain

Hannah Gibson has been living with chronic illness for most of her life. So why does she still struggle to get medical professionals to take her condition seriously? Before I found my current GP, I always had the urge to censor myself went I went to the doctor. To make my story palatable, less daunting. … Read more

The illness people can’t see: living with Chronic Fatigue Syndrome

What is it like to have a disease that nobody can ‘see’ and which society can shame you for talking about? To mark International ME/CFS Awareness Day, Hannah Gibson writes about her experience with ME/CFS, and the struggle to have her condition legitimised in Western medicine. When I was a young girl, my mother says … Read more